An inhomogeneous interface reaction in a liquid–liquid immiscible two-phase system is developed to realize the large-scale room-temperature synthesis of perovskite-related Cs4PbBr6 fluorophores.

Nitrogen-doped carbon dots with multi-state visible absorption and full-color blue/yellow/red emissions are synthesized, and show potential applications in solid-state-lighting.

Yb(3+)/Er(3+)/Cr(3+) triply doped transparent bulk glass ceramic containing orthorhombic YF3 and cubic Ga2O3 nanocrystals was fabricated by a melt-quenching route to explore its possible application in optical thermometry with high spatial and temperature resolution. It was experimentally observed that Yb(3+)/Er(3+) ions incorporated into the precipitated YF3 nanophase, while Cr(3+) ions partitioned into the crystallized Ga2O3 nanophase after glass crystallization. Importantly, such spatial isolation strategy efficiently suppressed adverse energy transfer among different active ions. As a consequence, intense green anti-Stokes luminescence originated from Er(3+): (2)H11/2,(4)S3/2 → (4)I15/2 transitions, and deep-red Stokes luminescence transitions assigned to Cr(3+): (2)E → (4)A2 radiation were simultaneously realized. Impressively, the intermediate crystal-field environment for Cr(3+) in Ga2O3 made it possible for lifetime-based temperature sensing owing to the competition of radiation transitions from the thermally coupled Cr(3+) (2)E and (4)T2 excited states. In the meantime, the low-phonon-energy environment for Er(3+) in YF3 was beneficial for upconversion fluorescence intensity ratio-based temperature sensing via thermal population between the (2)H11/2 state and (4)S3/2 state. The Boltzmann distribution theory and the two-level kinetic model were adopted to interpret these temperature-dependent luminescence of Er(3+) and Cr(3+), respectively, which gave the highest temperature sensitivities of 0.25% K(-1) at 514 K for Er(3+) and 0.59% K(-1) at 386 K for Cr(3+).

Dual-activator based optical thermometry with high sensitivity and superior signal discriminability was developed.

Full-color visible emissions are particularly crucial for applications in displays and lightings. In this work, we developed a facile room-temperature ligand-assisted supersaturated recrystallization synthesis of monodisperse, cubic structure CsFAPbX (X = Cl, Br, and I or their mixtures Cl/Br and Br/I, 0 ≤ m ≤ 1) hybrid perovskite quantum dots (QDs). Impressively, cation substitution of Cs by FA was beneficial in finely tuning the band gap and in exciton recombination kinetics, improving the structural stability, and raising the absolute quantum yields up to 85%. With further assistance of anion replacement, full-spectral visible emissions in the wavelength range of 450-750 nm; narrow full width at half-maxima, and a wide color gamut, encompassing 130% of National Television System Committee television color standard, were achieved. Finally, CsFAPbX-polymer films retaining multicolor luminescence are prepared and a prototype white light-emitting diode device was constructed using green CsFAPbBr and red CsFABrI QDs as color converters, certainly suggesting their potential applications in the optoelectronics field.

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A strategy to achieve high sensitivity of noncontact optical thermometer via the structure design of nanoglass-ceramic and the usage of Ln(3+) (Ln = Eu, Tb, Dy) luminescence as reference signal and Cr(3+) emission as temperature signal was provided. Specifically, the synthesized dual-phase glass-ceramics were evidenced to enable spatially confined doping of Ln(3+) in the hexagonal GdF3 nanocrystals and Cr(3+) in the cubic Ga2O3 nanoparticles, being beneficial to suppressing detrimental energy transfer between Ln(3+) and Cr(3+) and thus significantly enhancing their luminescence. As a consequence, completely different temperature-sensitive luminescence of Ln(3+)4f → 4f transition and Cr(3+) 3d → 3d transition in the present glass-ceramic resulted in obvious variation of Cr(3+)/Ln(3+) fluorescence intensity ratio with temperature and strikingly high detecting temperature sensitivity of 15-22% per K. We believe that this preliminary study will provide an important advance in exploring other innovative optical thermometry.

To circumvent the requirement of small energy gap between thermally coupled levels of lanthanide probes in optical thermometry, a strategy using dual-activator fluorescence intensity ratio as temperature signal in dual-phase nanostructural glass ceramics was reported. Specifically, oxyfluoride glass with specially designed composition of SiO 2 −Al 2 O 3 −LiF−EuF 3 −Ga 2 O 3 −Cr 2 O 3 was fabricated, and subsequently glass crystallization was used to induce homogeneous precipitation of hexagonal EuF 3 and cubic Ga 2 O 3 nanocrystals among the glass matrix. Impressively, Eu 2+ activators were produced after glass crystallization in an air atmosphere, and the Cr 3+ emitting center was evidenced to incorporate into Ga 2 O 3 crystalline lattice. As a result, temperature determination with high sensitivity of 0.8% K −1 , large energy gap of 8500 cm −1 , and superior thermal stability were realized by taking advantage of the fluorescence intensity ratio between Eu 2+ and Cr 3+ as detecting parameter, which exhibited a linear dependence on temperature. We believe that this preliminary investigation will provide a practical approach for developing a high-performance self-calibrated optical thermometer.